| Klippel-Trenaunay syndrome: a multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth. | |
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MedLine Citation:
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PMID: 16911369 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Klippel-Trenaunay syndrome is characterized by a triad of varicose veins, cutaneous capillary malformation, and hypertrophy of bone and soft tissue. Appropriate evaluation and treatment of children displaying features of the disease may minimize morbidity. The clinical appearance, etiology, genetics, diagnostics, and treatment of Klippel-Trenaunay syndrome are herein explored. |
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Authors:
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George G Kihiczak; Jon G Meine; Robert A Schwartz; Camila K Janniger |
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Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: International journal of dermatology Volume: 45 ISSN: 0011-9059 ISO Abbreviation: Int. J. Dermatol. Publication Date: 2006 Aug |
Date Detail:
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Created Date: 2006-08-16 Completed Date: 2007-01-10 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 0243704 Medline TA: Int J Dermatol Country: United States |
Other Details:
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Languages: eng Pagination: 883-90 Citation Subset: IM |
Affiliation:
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Dermatology and Pediatrics, New Jersey Medical School, Newark, NJ 07103-2714, USA. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Angiogenic Proteins
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genetics* Humans Klippel-Trenaunay-Weber Syndrome / diagnosis*, etiology, genetics*, therapy |
| Chemical | |
Reg. No./Substance:
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0/AGGF1 protein, human; 0/Angiogenic Proteins |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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